Evidence map›Paper›PMID 27119629›Full record

ReviewBiophysical journal2016

Optics-Integrated Microfluidic Platforms for Biomolecular Analyses.

Kathleen E Bates, Hang Lu

Open access · bronzeAbstract readReview
In one paragraph

Review in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Roadmap on optical sensors.Journal of optics (2010) · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Optofluidics Refractometers.Micromachines · 2018
    Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Kathleen E BatesInterdisciplinary Program in Bioengineering, Georgia Institute of Technology, Atlanta, Georgia; School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia.
Hang LuInterdisciplinary Program in Bioengineering, Georgia Institute of Technology, Atlanta, Georgia; School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia. Electronic address: hang.lu@gatech.edu.
Georgia Institute of Technology · US

Funding

Quantitative microscopy-based rapid phenotyping and screeningR01GM088333 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2011 to 2018
$2.3M
Quantitative Understanding of Mechnosensory Circuit on ChipR01NS096581 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2016 to 2020
$1.7M
Spatiotemporal control of reactive oxygen species in T cellsR01AI088023 · NIAID · GEORGIA INSTITUTE OF TECHNOLOGY · PI KEMP, MELISSA LAMBETH · 2011 to 2014
$1.4M
Automated droplet-based platform for combinatorial screens on whole animalsR21EB021676 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2015 to 2016
$429k
Evolving multigenic extensions to lifespanR21AG050304 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG, MCGRATH, PATRICK T · 2015 to 2016
$391k
Spatiotemporal control of reactive oxygen species in T cellsR56AI088023 · NIAID · GEORGIA INSTITUTE OF TECHNOLOGY · PI KEMP, MELISSA LAMBETH, LU, HANG · 2015 to 2015
$371k
NIAID NIH HHS R01 AI088023NIAID NIH HHS R56 AI088023NIA NIH HHS R21 AG050304NIBIB NIH HHS R21 EB021676NIGMS NIH HHS R01 GM088333NINDS NIH HHS R01 NS096581
6 · The paper itself

Abstract

Compared with conventional optical methods, optics implemented on microfluidic chips provide small, and often much cheaper ways to interrogate biological systems from the level of single molecules up to small model organisms. The optical probing of single molecules has been used to investigate the mechanical properties of individual biological molecules; however, multiplexing of these measurements through microfluidics and nanofluidics confers many analytical advantages. Optics-integrated microfluidic systems can significantly simplify sample processing and allow a more user-friendly experience; alignments of on-chip optical components are predetermined during fabrication and many purely optical techniques are passively controlled. Furthermore, sample loss from complicated preparation and fluid transfer steps can be virtually eliminated, a particularly important attribute for biological molecules at very low concentrations. Excellent fluid handling and high surface area/volume ratios also contribute to faster detection times for low abundance molecules in small sample volumes. Although integration of optical systems with classical microfluidic analysis techniques has been limited, microfluidics offers a ready platform for interrogation of biophysical properties. By exploiting the ease with which fluids and particles can be precisely and dynamically controlled in microfluidic devices, optical sensors capable of unique imaging modes, single molecule manipulation, and detection of minute changes in concentration of an analyte are possible.

Indexed as

Optical PhenomenaAnimalsHumansInterferometryMicrofluidic Analytical TechniquesSpectrum Analysis

Identifiers

PMID27119629
PMCPMC4850344
OpenAlexW2345123838

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.